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Changes in the gut microbiota of cloned and non-cloned control pigs during development of obesity: gut microbiota during development of obesity in cloned pigs

机译:在肥胖症发育过程中克隆和非克隆对照猪的肠道微生物的变化:肠道猪肥胖症的发展过程中的肠道微生物

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Background Obesity induced by a high-caloric diet has previously been associated with changes in the gut microbiota in mice and in humans. In this study, pigs were cloned to minimize genetic and biological variation among the animals with the aim of developing a controlled metabolomic model suitable for a diet-intervention study. Cloning of pigs may be an attractive way to reduce genetic influences when investigating the effect of diet and obesity on different physiological sites. The aim of this study was to assess and compare the changes in the composition of the gut microbiota of cloned vs. non-cloned pigs during development of obesity by a high-fat/high-caloric diet. Furthermore, we investigated the association between diet-induced obesity and the relative abundance of the phyla Firmicutes and Bacteroidetes in the fecal-microbiota. The fecal microbiota from obese cloned (n = 5) and non-cloned control pigs (n= 6) was investigated biweekly over a period of 136 days, by terminal restriction fragment length polymorphism (T-RFLP) and quantitative real time PCR (qPCR). Results A positive correlation was observed between body-weight at endpoint and percent body-fat in cloned (r=0.9, PPFirmicutes in both cloned (r=0.37; PPBacteroidetes in cloned pigs (r=?0.33, P Conclusion The cloned pigs did not have reduced inter-individual variation as compared to non-cloned pigs in regard to their gut microbiota in neither the obese nor the lean state. Diet-induced obesity was associated with an increase in the relative abundance of Firmicutes over time. Our results suggest that cloned pigs are not a more suitable animal model for gut microbiota-obesity related studies than non-cloned pigs. This study is the first to evaluate if cloned pigs provide a better animal model than conventional pigs in diet-intervention, obesity and gut microbiota research.
机译:高热量饮食引起的背景肥胖以前与小鼠和人类中肠道微生物群的变化有关。在该研究中,克隆猪以最小化动物之间的遗传和生物变异,目的是开发适合饮食干预研究的受控代谢组型。在研究饮食和肥胖对不同生理位点的影响时,猪的克隆可能是一种有吸引力的方式来减少遗传影响。本研究的目的是评估并比较克隆与非克隆猪的肠道微生物的组成的变化在肥胖的肥胖期间通过高脂/高热量饮食。此外,我们调查了饮食诱导的肥胖症与粪便微生物中的饮食肥胖症和诸如植物的相对丰富的关系。通过末端限制性片段长度多态性(T-RFLP)和定量实时PCR(QPCR,来自肥胖克隆(n = 5)和非克隆对照猪(n = 6)的粪便微生物(n = 6)和非克隆对照猪(n = 6)。 )。结果在克隆的终点和体脂百分比之间观察到阳性相关性(克隆(r = 0.37;克隆猪中的pp ercirmetes(r = @ 0.33),r = 0.9,ppα10.33,p结论克隆猪没有与肥胖的肥胖的肠道或贫瘠的猪中的非克隆猪相比,在单个肠道猪中没有减少单独的变化。饮食诱导的肥胖与随着时间的推移相对丰富的反应增加。我们的结果表明克隆的猪不是更合适的动物模型,用于肠道微生物脂肪肥胖相关的研究,而不是非克隆猪。该研究是第一个评价克隆猪提供比饮食干预,肥胖和肠道微生物症研究更好的动物模型。 。

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